James C. Mullikin

Computational Biology & Bioinformatics · 2001–2020

A researcher in the Science corpus: 22 papers; trusts 5 researchers and is trusted by 15 researchers here, as inferred from the citation graph.

Subfields

• Computational Biology & Bioinformatics — 26 citations into it

Whom James C. Mullikin trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. Donald Ervin Knuth
2. Stephen F. Altschul
3. Temple F. Smith

Who trusts James C. Mullikin overall

1. Heng Li
2. Robert Schmieder
3. Jay Shendure

Papers from James C. Mullikin's perspective

Ordered by how strongly the researchers James C. Mullikin trusts endorse each paper. Same corpus, a different order for every researcher.

1. Basic local alignment search tool.
2. Initial sequencing and comparative analysis of the mouse genome (Nature)
3. An SNP map of the human genome generated by reduced representation shotgun sequencing (Nature)
4. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice.
5. The microRNAs of Caenorhabditis elegans. (Genes & Development)
6. Personalized Copy-Number and Segmental Duplication Maps using Next-Generation Sequencing (Nature Genetics)
7. A Draft Sequence of the Rice Genome (Oryza sativa L. ssp. japonica) (Science)
8. The Pfam protein families database
9. Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
10. Genetic analyses from ancient DNA. (Annual Review of Genetics)

Their papers

• Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (2008) — 3,840 citations
• Initial sequencing and analysis of the human genome (2001) — 24,262 citations
• SSAHA: a fast search method for large DNA databases. (2001) — 1,044 citations
• The Genome Sequence of Caenorhabditis briggsae: A Platform for Comparative Genomics (2003) — 1,019 citations
• A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
• A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms (2001) — 2,947 citations
• Initial sequencing and comparative analysis of the mouse genome. (2002) — 4,291 citations
• A robust benchmark for detection of germline large deletions and insertions (2020) — 358 citations
• Telomere-to-telomere assembly of a complete human X chromosome (2019) — 617 citations
• The DNA sequence of the human X chromosome (2005) — 1,099 citations
• Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease (2020) — 871 citations
• Developmental Pathway of the MPER-Directed HIV-1-Neutralizing Antibody 10E8 (2016) — 49 citations
• Quantifying B cells capable of producing broadly neutralizing antibodies against influenza serves as a metric to guide the development of a universal influenza vaccine (2016)
• Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2 (2014) — 757 citations
• Developmental pathway for potent V1V2-directed HIV-neutralizing antibodies (2014) — 742 citations
• Great ape genetic diversity and population history (2013) — 858 citations
• The complete genome sequence of a Neandertal from the Altai Mountains (2013) — 1,650 citations
• The genome of the ctenophore Mnemiopsis leidyi and its implications for cell type evolution (2013) — 665 citations
• Co-evolution of a broadly neutralizing HIV-1 antibody and founder virus (2013) — 1,030 citations
• Focused Evolution of HIV-1 Neutralizing Antibodies Revealed by Structures and Deep Sequencing (2011) — 757 citations